Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and HBB[original query] |
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Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia. British journal of haematology 2013 Oct 163 (2): 268-76. Bean Christopher J, Boulet Sheree L, Yang Genyan, Payne Amanda B, Ghaji Nafisa, Pyle Meredith E, Hooper W Craig, Bhatnagar Pallav, Keefer Jeffrey, Barron-Casella Emily A, Casella James F, Debaun Michael |
Functional polymorphisms of BCL11A and HBS1L-MYB genes affect both fetal hemoglobin level and clinical outcomes in a cohort of children with sickle cell anemia. Annals of hematology 2020 May . Sales Rahyssa Rodrigues, Belisário André Rolim, Faria Gabriela, Mendes Fabiola, Luizon Marcelo Rizzatti, Viana Marcos Bora |
Hb S/?-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics. Hemoglobin 2020 3 44 (1): 1-9. Belisário André R, Carneiro-Proietti Anna B, Sabino Ester Cerdeira, Araújo Aderson, Loureiro Paula, Máximo Cláudia, Flor-Park Miriam V, Rodrigues Daniela D O W, Ozahata Mina Cintho, McClure Christopher, Mota Rosimere Afonso, Gomes Moura Isabel C, Custer Brian, Kelly Shannon, |
Determination of Carrier Frequency of Actionable Pathogenic Variants in Autosomal Recessive Genetic Diseases in the Turkish Cypriot Population. Genes 2023 10 14 (10): . Aziz Suat Gunsel, Mahmut Cerkez Ergoren, Hatice Kemal, Haniyeh Rahbar Kafshboran, Levent Cerit, Ayla Turgay, Hamza Duy |
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